Chemical Formula | C6H4BrF |
Molar Mass | 175.00 g/mol |
Appearance | Colorless to light yellow liquid |
Boiling Point | 154 - 156 °C |
Melting Point | -35 °C |
Density | 1.578 g/mL at 25 °C |
Solubility In Water | Insoluble |
Solubility In Organic Solvents | Soluble in common organic solvents like ethanol, ether |
Flash Point | 49 °C |
Odor | Characteristic aromatic odor |
Cas Number | 460-00-4 |
Name | 4-Bromo-1-fluorobenzene |
Molecular Formula | C6H4BrF |
Molecular Weight | 175.00 |
Appearance | Colorless to light yellow liquid |
Boiling Point | 154 - 156 °C |
Melting Point | -27 °C |
Density | 1.57 g/cm³ |
Flash Point | 46 °C |
Solubility In Water | Insoluble |
Vapor Pressure | 1.33 kPa (34.3 °C) |
Refractive Index | 1.5455 |
Name | 4-Bromo-1-fluorobenzene |
Molecular Formula | C6H4BrF |
Molecular Weight | 175.00 |
Cas Number | 460-00-4 |
Appearance | Colorless to light yellow liquid |
Boiling Point | 154 - 156 °C |
Melting Point | -27 °C |
Density | 1.57 g/mL at 25 °C |
Flash Point | 47 °C |
Solubility | Insoluble in water, soluble in organic solvents |
Odor | Characteristic aromatic odor |
What are the main uses of 4-Bromo-1-fluorobenzene?
4-Bromo-1-fluorobenzene is also an organic compound. It has a wide range of uses and has important applications in many fields.
First, it is often a key intermediate in the synthesis of medicine. Due to the unique properties of bromine and fluorine atoms, it can participate in a variety of chemical reactions and help build complex drug molecular structures. For example, when synthesizing specific antibacterial drugs, 4-bromo-1-fluorobenzene can undergo a series of reactions to introduce specific functional groups to shape the activity check point of the drug and make it have antibacterial effect.
Second, it also plays an important role in the field of materials science. It can be used as a basic raw material in the preparation of high-performance organic optoelectronic materials. With the electronegativity of fluorine atoms and the appropriate steric resistance of bromine atoms, the electron transport properties and optical properties of materials can be regulated. The resulting materials can be used in organic Light Emitting Diodes (OLEDs) to improve their luminous efficiency and stability; or in solar cells to enhance the absorption of light and charge transport, thereby improving the conversion efficiency of batteries.
Third, in the synthesis of pesticides, 4-bromo-1-fluorobenzene is also indispensable. After chemical modification, pesticides with high insecticidal and bactericidal properties can be created. Due to its unique structure, it can precisely act on specific targets of pests or pathogens, achieve the purpose of efficient control, and have a relatively small impact on the environment, which is in line with the development trend of modern green pesticides.
In summary, 4-bromo-1-fluorobenzene, with its unique chemical structure, plays a key role in the fields of medicine, materials, pesticides, etc., and promotes technological progress and industrial development in various fields.
What are the physical properties of 4-Bromo-1-fluorobenzene?
4-Bromo-1-fluorobenzene is also an organic compound. It has special physical properties and is widely used in various fields of chemical industry.
In terms of its properties, under room temperature, 4-bromo-1-fluorobenzene is colorless to light yellow liquid, and it looks clear and transparent. It has a certain volatility and can slowly dissipate in the air. Smell it, it has a specific smell, but it is not pungent and intolerable, but it is more unique to the ear.
When it comes to the melting point, the melting point of this compound is about -27 ° C. At this temperature, 4-bromo-1-fluorobenzene gradually converts from liquid to solid, and the molecular arrangement tends to be orderly. The boiling point is about 154-156 ° C. When the temperature rises to the boiling point, the liquid absorbs enough energy, the thermal motion of the molecules intensifies, overcomes the intermolecular forces, changes from liquid to gaseous state, and escapes into the air.
The density of 4-bromo-1-fluorobenzene is heavier than that of water, about 1.716g/cm ³. Therefore, if it is mixed with water, it will sink to the bottom of the water, and the two are difficult to dissolve each other due to polar differences. This compound is soluble in many organic solvents, such as ethanol, ether, dichloromethane, etc. With a similar degree of miscibility, it is similar to the intermolecular forces of organic solvents, so it is miscible.
In addition, the vapor pressure of 4-bromo-1-fluorobenzene has a certain value at a specific temperature. The vapor pressure is related to its degree of volatilization. The higher the vapor pressure, the more volatile it is under the same conditions. Its refractive index is also a specific value, and this property can be used for identification and purity analysis. Cover 4-bromo-1-fluorobenzene of different purity, the refractive index is slightly different, and it can be measured by precision instruments to identify its purity.
What is the chemistry of 4-Bromo-1-fluorobenzene?
4-Bromo-1-fluorobenzene is also an organic compound. In its molecular structure, above the benzene ring, the bromine atom and the fluorine atom are separated from the para-position. The chemical properties of this substance are very interesting and are important in the field of organic synthesis.
In terms of its reactivity, the electron cloud density of the benzene ring changes due to the substitution of bromine and fluorine. Fluorine atoms are extremely electronegative and have a strong electron-absorbing induction effect, which reduces the electron cloud density of the benzene ring, and the electrophilic substitution reaction is more difficult than that of benzene. However, the electron cloud density of the adjacent and para-position is relatively higher, and the electrophilic reagents can still attack the adjacent and para-position. Although bromine atoms also have electron-absorbing induction effects, they have both electron-giving conjugation effects, which generally reduce the electron cloud density of the benzene ring less than that of fluorine, and also affect the check point of electrophilic substitution reactions.
In electrophilic substitution reactions, halogenation, nitrification, sulfonation, etc. may occur. For example, during nitrification, nitro groups tend to enter the adjacent and para-sites of bromine. In addition, 4-bromo-1-fluorobenzene can participate in metal-catalyzed coupling reactions. Such as with organometallic reagents, under the action of metal catalysts such as palladium and nickel, carbon-carbon bonds and carbon-hetero bonds can be formed. This reaction is especially important for the construction of complex organic molecular structures, which can synthesize organic materials with specific functions, pharmaceutical intermediates, etc.
The chemical properties of 4-bromo-1-fluorobenzene are determined by their structure, and play a key role in many fields of organic synthesis. With their unique reactivity, chemists can create a variety of organic compounds and promote the development of organic chemistry and related industries.
What are 4-Bromo-1-fluorobenzene synthesis methods?
There are several methods for the synthesis of 4-bromo-1-fluorobenzene.
First, benzene is used as the starting material. First, benzene is brominated, and bromine and an appropriate catalyst, such as iron powder, can be obtained at a suitable temperature. This reaction mechanism is that the bromine molecule is polarized under the action of the catalyst to form a positive bromide ion, which attacks the benzene ring and undergoes an electrophilic substitution reaction. Then, the bromobenzene is nitrified. In a mixed acid of concentrated nitric acid and concentrated sulfuric acid, the bromobenzene is introduced into the nitro group at a specific temperature range to obtain p-bromonitrobenzene. Due to the fact that bromine is an ortho-para-locator and the influence of space steric resistance, the nitro group mainly enters the para-site. Then, p-bromo-nitrobenzene is reduced, and the nitro group can be converted into an amino group with suitable reducing agents such as iron and hydrochloric acid to obtain p-bromo-aniline. Subsequently, p-bromo-aniline is diazotized with sodium nitrite and hydrofluoric acid at low temperature, and the amino group is converted into diazonium salt. After treatment with fluoroboronic acid, the diazonium group is replaced by fluorine atoms, and finally 4-bromo-1-fluorobenzene is obtained.
Second, starting from p-bromo-phenol. Under appropriate solvent and reaction conditions, the hydroxyl group of p-bromo-phenol and fluorinated reagents, such as potassium fluoride, can be replaced by fluorine atoms to obtain the target product 4-bromo-1-fluorobenzene. This reaction requires specific conditions to promote the smooth progress of nucleophilic sub
Third, use 1,4-dihalobenzene derivatives as raw materials. If there is 1,4-dibromobenzene, 4-bromo-1-fluorobenzene can be prepared by halogen exchange reaction with metal fluorides, such as zinc fluoride, under suitable reaction systems and conditions, so that one of the bromine atoms is replaced by a fluorine atom. In this process, the reaction conditions have a great influence on the reaction selectivity and yield.
The above synthesis methods have their own advantages and disadvantages, and should be selected according to actual needs and conditions, such as raw material availability, cost, reaction difficulty and other factors.
What are the precautions in storage and transportation of 4-Bromo-1-fluorobenzene?
4-Bromo-1-fluorobenzene is an organic compound. When storing and transporting, you must pay attention to many matters to prevent accidents and ensure safety.
First, when storing, you should choose a cool and ventilated warehouse. This compound is easy to decompose when heated. If the warehouse temperature is too high, it may cause a decomposition reaction and cause danger. And good ventilation can allow the gas that may leak to be discharged in time, reduce the concentration of accumulation, and avoid the risk of explosion and poisoning.
Second, keep away from fire and heat sources. 4-Bromo-1-fluorobenzene is flammable, and it is easy to burn or even explode in case of open flames and hot topics. Therefore, fireworks are strictly prohibited inside and outside the warehouse, and electrical equipment must also have explosion-proof functions.
Third, it should be stored separately from oxidants and edible chemicals. Because of its contact with oxidants or violent chemical reactions, it is dangerous; stored with edible chemicals, if leaked, it is easy to contaminate food and endanger human health.
Fourth, the storage container must be sealed. 4-Bromo-1-fluorobenzene is volatile. A sealed container can prevent volatilization, ensure material quality, reduce environmental impact, and avoid safety hazards caused by the accumulation of volatile gases.
As for transportation, transportation vehicles must be equipped with corresponding varieties and quantities of fire equipment and leakage emergency treatment equipment. In case of fire and other emergency situations on the way, it can be put out in time. And the transportation process should be protected from exposure to sun, rain, and high temperature.
When loading and unloading, it should also be handled lightly to prevent damage to packaging and containers. If the packaging is damaged, 4-bromo-1-fluorobenzene leaks, which not only loses materials, but also pollutes the environment and endangers the safety of personnel.
To sum up, 4-bromo-1-fluorobenzene must be operated in strict accordance with regulations in storage and transportation, from the warehouse selection, away from the fire source, to the sealing of the container, transportation protection, loading and unloading attention, etc., to ensure the safety of personnel, the environment and the material itself.